US6746618B2 - Electro-optic ceramic material and device - Google Patents

Abstract

The present invention provides an electro-optic ceramic material including lead, zinc and niobium having a propagation loss of less than about 3 dB/cm and a quadratic electro-optic coefficient of greater than about 1×10⁻⁶ m²/V² at 20° C. at a wavelength of 1550 nm. The present invention also provides electro-optic devices including an electro-optic ceramic material including lead, zinc and niobium having a propagation loss of less than about 3 dB/cm and a quadratic electro-optic coefficient of greater than about 1×10⁻¹⁶ m² V at 20° C. at a wavelength of 1550 nm. The materials and devices of the present invention are useful in optical communications applications such as intensity and phase modulation, switching, and polarization control.

Description

BACKGROUND OF THE INVENTION

1. Field of the Invention

The present invention relates to materials and devices for optical communications, and more particularly to electro-optic ceramic materials having high transparency and electro-optic activity and devices constructed using such materials.

2. Technical Background

While much progress has been made in the last thirty years in developing optical switches or modulators, current devices are not satisfactory for every application. Many active optical devices, such as intensity attenuators, used in present-day systems are based on electromechanical actuation. In one type of conventional device, optical fibers are positioned end to end and mechanically moved into or out of line. In another type of conventional device, mirrors are rotated to direct beams into or away from a receiving fiber. This can be accomplished mechanically, or with piezoelectric or electrostatic devices. Devices based on motion of components have slow switching times, and may have unacceptable environmental or long-term stability.

Optical devices without moving parts have been designed to address some of the switching speed and stability problems mentioned above. These devices depend on materials that can change optical properties without bulk motion, such as liquid crystals and electro-optic crystal materials. Liquid crystals tend to have relatively slow switching speeds, as the mechanism of actuation is rotation of entire molecules under the influence of an electric field. Electro-optic crystal materials such as LiNbO₃ have much higher switching speeds, but are extremely polarization dependent.

One especially promising class of materials for use in active optical devices is electro-optic ceramic materials. Electro-optic ceramic materials are generally composed of ferroelectric complex oxides, and are polycrystalline. Due to the random orientations of the individual crystalline grains, electro-optic ceramic materials are optically isotropic in the absence of an electric field. In the presence of an electric field, electro-optic ceramic materials become anisotropic, with a lower refractive index in the direction of the field than perpendicular to the field. These materials may be switched between isotropic and anisotropic states by controlling the electric field. For use in electro-optic applications, it is desirable that electro-optic ceramic materials have high transparency, high quadratic electro-optic coefficients and low switching hysteresis.

Lead lanthanum zirconate titanate (PLZT) is the most common electro-optic ceramic material. PLZT materials can be formed to be substantially transparent to light having wavelengths in the range of 0.5 μm to 7 μm. Properties of PLZT compositions can be tuned by adjusting the relative amounts of lead, lanthanum, zirconate and titanate. For example, a PLZT composition having the formula Pb_0.91La_0.9(Zr_0.65Ti_0.35)_0.9775O₃ has a quadratic electro-optic coefficient R=9.2×10⁻¹⁶ m²/V², but has extremely high hysteresis in its switching behavior as well as poor temperature stability, making it unsuitable for high-speed electro-optic applications. By increasing the lanthanum concentration, one can improve hysteresis at the expense of electro-optic activity. For example, a PLZT composition having the formula Pb_0.9025La_0.0975(Zr_0.65Ti_0.35)_0.975625O₃ has a lower quadratic electro-optic coefficient (R˜2.5×10⁻⁶ m²/V² at room temperature), but has temperature stability and hysteresis suitable for use in devices for optical telecommunications. PLZT materials also suffer from high brittleness and low toughness. Attempts to find new electro-optic ceramics have generally failed to provide an electro-optic ceramic material that has high transparency, a high quadratic electro-optic coefficient, and low hysteresis.

SUMMARY OF THE INVENTION

One embodiment of the present invention relates to an electro-optic ceramic material including lead, zinc and niobium, wherein the electro-optic material has a propagation loss of less than about 3 dB/cm and a quadratic electro-optic coefficient of greater than about 1×10⁻¹⁶ m² V² at 20° C. at a wavelength of 1550 nm.

Another embodiment of the present invention relates to an electro-optic ceramic material including lead, zinc and niobium, wherein the electro-optic material has a propagation loss of less than about 3 dB/cm and a quadratic electro-optic coefficient of greater than about 1×10⁻⁶ m² V² at 20° C. at a wavelength of 1550 nm, and wherein the electro-optic ceramic material further includes titanium, wherein the electro-optic ceramic material has a lead cation fraction of between about 0.20 and about 0.50; a barium cation fraction of less than about 0.26; a lanthanum cation fraction of less than about 0.05; a zinc cation fraction of between about 0.07 and about 0.17; a niobium cation fraction of between about 0.15 and about 0.33; and a titanium cation fraction of between about 0.03 and about 0.27.

Another embodiment of the present invention relates to an electro-optic ceramic material including lead, zinc and niobium, wherein the electro-optic material has a propagation loss of less than about 3 dB/cm and a quadratic electro-optic coefficient of greater than about 1×10⁻¹⁶ m²/V² at 20° C. at a wavelength of 1550 nm, and wherein the electro-optic ceramic material has the formula Pb_1−y−zBa_yLa_z[(Zn_tNb_1−t)_xTi_1−x]_1−z/4O_{3+x/2−3xt/2−xz/8+3+xtz/8}, wherein x is between about 0.5 and about 0.9, y is between about 0.05 and about 0.5, z is between about 0 and about 0.05, and t is between about 0.30 and about 0.36.

Another embodiment of the present invention relates to an electro-optic device including an electro-optic ceramic material including lead, zinc and niobium, wherein the electro-optic ceramic material has a propagation loss of less than about 3 dB/cm and a quadratic electro-optic coefficient of greater than about 1×10⁻⁶ m²/V² at 20° C. a wavelength of 1550 nm.

Another embodiment of the present invention relates to an electro-optic device including an electro-optic ceramic material including lead, zinc and niobium, wherein the electro-optic ceramic material has a propagation loss of less than about 3 dB/cm and a quadratic electro-optic coefficient of greater than about 1×10⁻⁶ m²/V² at 20° C. at a wavelength of 1550 nm, wherein the electro-optic ceramic material further comprises titanium, and wherein the electro-optic ceramic material has a lead cation fraction of between about 0.20 and about 0.50; a barium cation fraction of less than about 0.26; a lanthanum cation fraction of less than about 0.05; a zinc cation fraction of between about 0.07 and about 0.17; a niobium cation fraction of between about 0.15 and about 0.33; and a titanium cation fraction of between about 0.03 and about 0.27.

The materials and devices of the present invention result in a number of advantages over conventional materials and devices. The materials of the present invention have high transparency over a wide wavelength range as well as high quadratic electro-optic coefficients. The materials of the present invention require a lower temperature for fabrication than does PLZT. The materials of the present invention have low hysteresis, making them suitable for use in electro-optic devices for telecommunications applications. Additional features and advantages of the invention will be set forth in the detailed description which follows, and in part will be readily apparent to those skilled in the art from the description or recognized by practicing the invention as described in the written description and claims hereof, as well as in the appended drawings.

It is to be understood that both the foregoing general description and the following detailed description are merely exemplary of the invention, and are intended to provide an overview or framework to understanding the nature and character of the invention as it is claimed.

The accompanying drawings are included to provide a further understanding of the invention, and are incorporated in and constitute a part of this specification. The drawings are not necessarily to scale. The drawings illustrate one or more embodiment(s) of the invention, and together with the description serve to explain the principles and operation of the invention.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a schematic depiction of a general perovskite structure;

FIG. 2 is an X-ray diffraction spectrum of an undensified powder of an embodiment of the present invention;

FIG. 3 is a schematic diagram of a hot pressing setup used to fabricate the electro-optic ceramics of the present invention;

FIG. 4 is a transmission spectrum of an electro-optic ceramic material of one embodiment of the present invention;

FIG. 5 is a graph of dielectric constants at different frequencies and temperatures for an electro-optic ceramic material of the present invention;

FIG. 6 is a schematic diagram of an experimental setup used to measure electro-optic coefficients;

FIG. 7 is a diagram graphically showing the compositions of Example 3;

FIG. 8 is a transmission spectrum of two electro-optic compositions of one embodiment of the present invention; and

FIG. 9 is a graph of electro-optic coefficient versus temperature for an electro-optic ceramic material of one embodiment of the present invention.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

The present invention provides an electro-optic ceramic material with high transparency, high quadratic electro-optic coefficients, and low hysteresis. The electro-optic ceramic materials of the present invention are lead zinc niobate-based ceramics having a propagation loss of less than about 3 dB/cm and a quadratic electro-optic coefficient of greater than about 1×10⁻⁶ m²/V² at 20° C. at a wavelength of 1550 nm. The electro-optic ceramic materials of the present invention are useful in the fabrication of electro-optic devices such as modulators, switches, phase retarders, polarization controllers, and variable optical attenuators.

Electro-optic materials are materials that change their birefringence in the presence of an electric field. The utility of an electro-optic material in an electro-optic device depends, in large part, on the magnitude of its electro-optic coefficients. The birefringence Δn of an electro-optic material in the presence of an electric field can be described by the equation $\Delta n=\Delta {\mathrm{<figure-callout\; id="0"\; label="n"\; filenames="US06746618-20040608-D00000.png,US06746618-20040608-D00002.png"\; state="\{\{state\}\}">n</figure-callout>}}_0+\frac{n^3}{2}\left(\gamma ·E+R·E^2\right)$

where Δn₀ is the birefringence of the material in the absence of an electric field, n is the ordinary refractive index of the material, E is the magnitude of the applied electric field, γ is the linear electro-optic coefficient, and R is the quadratic electro-optic coefficient. As the electro-optic ceramic materials of the present invention are isotropic, Δn₀ and y are essentially zero, making the electro-optic activity proportional to the quadratic electro-optic coefficient. The lead zinc niobate electro-optic ceramic materials described herein have quadratic electro-optic coefficients R at 20° C. at a wavelength of 1550 nm of greater than about 1×10⁻¹⁶ m²/V², and preferably greater than about 3×10⁻¹⁶ m²/V².

While electro-optic activity is important, a material with high electro-optic activity will be rendered useless if it is not sufficiently transparent at the wavelength of interest. Transparency at telecommunications wavelengths is an important feature of the electro-optic ceramic materials of the present invention. As will be described more fully below, the electro-optic ceramic materials of the present invention can be formed by the skilled artisan to be very dense and relatively free of scattering voids and undesired impurity phases. The electro-optic ceramic materials of the present invention have propagation losses of less than about 3 dB/cm, and preferably less than about 1.5 dB/cm, and more preferably less than about 1.0 dB/cm at 1550 nm.

In one aspect of the present invention, the electro-optic ceramic material includes lead, zinc, niobium and titanium, and preferably includes barium and/or lanthanum. The relative amounts of individual atomic species may be described by a cation fraction. As used herein, a cation is any atomic species bearing a positive formal charge. For example, though the titanium atom is part of the polyatomic titanium anion (TiO₃ ²⁻) in the present compositions, the titanium atom itself has a +4 formal charge, and is thus considered herein to be a cation. The cation fraction of a particular atomic species is the ratio of the number of atoms of the particular atomic species to the total number of cationic atoms. For example, for the electro-optic ceramic material

Pb_0.83Ba_0.15La_0.02[(Zn_1/3Nb_2/3)_0.7Ti_0.3]_0.995O₃,

the cation fractions may be calculated as follows:

Lead cation fraction=0.83/[0.83+0.15+0.02+((⅓+⅔)·0.7+0.3)·0.995]=0.416

Barium cation fraction=0.15/[0.83+0.15+0.02+((⅓+⅔)·0.7+0.3)·0.995]=0.075

Lanthanum cation fraction=0.02/[0.83+0.15+0.02+((⅓+⅔)·0.7+0.3)·0.995]=0.010

Zinc cation fraction=[⅓·0.7·0.995]/[0.83+0.15+0.02+((⅓+⅔)·0.7+0.3)·0.995]0.116

Niobium cation fraction=[⅔·0.7·0.995]/[0.83+0.15+0.02+((⅓+⅔)·0.7+0.3)·0.995]=0.232

Titanium cation fraction=[0.3·0.995]/[0.83+0.15+0.02+((⅓+⅔)·0.7+0.3)·0.995]=0.150

In preferred embodiments of the present invention, the electro-optic ceramic material has a lead cation fraction of between about 0.20 and about 0.50, a barium cation fraction of less than about 0.26, a lanthanum cation fraction of less than about 0.05, a zinc cation fraction of between about 0.07 and about 0.17, a niobium cation fraction of between about 0.15 and about 0.33, and a titanium cation fraction of between about 0.03 and about 0.27. The electro-optic ceramic material may have a lead cation fraction of between about 0.37 and about 0.45. The electro-optic ceramic material may have a barium cation fraction of between about 0.04 and about 0.11. The electro-optic ceramic material may have lanthanum cation fraction of between about 0.01 and about 0.04. The electro-optic ceramic material may have a zinc cation fraction of between about 0.10 and about 0.15. The electro-optic ceramic material may have a niobium cation fraction of between about 0.20 and about 0.29. The electro-optic ceramic material may have a titanium cation fraction of between about 0.07 and about 0.18.

In the electro-optic ceramic materials of the present invention, each crystalline grain desirably has a perovskite structure. The perovskite structure, shown in FIG. 1, has a unit cell in which the large cations (e.g. Pb²⁺, La³⁺, Ba²⁺) and the anions (e.g. O²⁻) form a cubic close packed (ccp) array with the smaller cations (e.g. Zn²⁺, Nb⁵⁺, Ti⁴⁺) occupying those octahedral holes formed exclusively by anions. In order to stabilize the desired perovskite phase of the lead zinc niobate electro-optic ceramic material, it may be desirable to include barium with a barium cation fraction of between about 0.03 and about 0.26. Alternatively, the skilled artisan may use other perovskite-stabilizing elements familiar to the skilled artisan. In order to improve thermal stability, density, isotropy and electro-optic activity of the electro-optic ceramic material, it may be desirable to include lanthanum with a lanthanum cation fraction of between about 0.005 and about 0.05. Small amounts of other cations may be included in the electro-optic ceramics of the present invention in order to further tune the properties according to methods familiar to the skilled artisan.

Preferred electro-optic ceramics of the present invention may be described by the general formula

Pb_1−y-zBa_yLa_z[(Zn_tNb_1−t)_xTi_1−x]_1−z/4O_{3+x/2−3xt/2−xz/8+3xtz/8}

wherein x is between about 0.5 and about 0.9, y is between about 0.05 and about 0.5, z is between about 0 and about 0.05, and t is between about 0.30 and about 0.36. In especially preferred electro-optic ceramic materials of the present invention, x is between about 0.65 and about 0.85, y is between about 0.1 and about 0.2, z is between about 0.02 and 0.04, and t is between about 0.32 and about 0.34.

The electro-optic ceramic materials of the present invention may be made by methods familiar to the skilled artisan. A wide variety of inorganic compounds may be used as the starting materials. For example, oxides, hydroxides, carbonates, sulfates, acetates or alkoxides of the desired metals may be used to form the ceramics of the present invention. In general, an opaque powder having the desired ceramic stoichiometry is first prepared and dried. For example, the mixed oxide method has been used to fabricate powders of the materials of the present invention, as described below in Example 1. Other methods, such as chemical co-precipitation and other more advanced techniques, may be used to prepare the powder. Before being densified, the powder may optionally be formed into an opaque powder preform by, for example, cold pressing.

The opaque powder or powder preform may then densified by methods familiar to the skilled artisan to form the ceramic materials of the present invention. For example, a powder preform may be hot-pressed to form a dense, transparent, perovskite-structured ceramic as described below in Example 1. Important processing parameters such as hot-pressing temperature, applied pressure, ambient conditions and processing time may be determined by the skilled artisan. Other densification techniques, such as vacuum sintering, isostatic pressing, hot isostatic pressing, or other pressing or sintering methods may be used by the skilled artisan to form the transparent ceramics of the present invention.

Hysteresis is the dependence of the state of a material on the history of an externally modified parameter. For example, in a electro-optic ferroelectric material exhibiting large hysteresis, a field-induced state (e.g. polarization, birefringence) depends not only on the magnitude of the field, but also on the history of the field (e.g. rate of field increase or decrease). The electro-optic ceramic materials of the present invention have very little hysteresis. In these materials, hysteresis is a measure of the work required to displace the ferroelectric domain walls in the material. The hysteresis is closely related both to the defect distribution in the crystal and to the energy barrier separating the different orientational states. High hysteresis is desirable for optical memory devices, while low hysteresis is desirable for optical modulation and switching applications. It is especially desirable for an electro-optic ceramic material to have low hysteresis at room temperature so that devices may be operated without feedback control or external heating. The materials of the present invention exhibit a so-called “slim loop” hysteresis behavior.

The electro-optic ceramic materials of the present invention are useful in the construction of electro-optic devices for telecommunications. Another aspect of the invention is an electro-optic device including a lead zinc niobate-based electro-optic ceramic material having a propagation loss of less than about 3 dB/cm and a quadratic electro-optic coefficient of greater than about 1×10¹⁶ m²/V² at 20° C. at a wavelength of 1550 nm. The electro-optic material preferably has a propagation loss of less than about 1.5 dB/cm, and a quadratic electro-optic coefficient at 20° C. of greater than about 3×10⁻¹⁶ m²/V². The electro-optic ceramic material used in the device may have the compositions described hereinabove. The electro-optic ceramic material may have, for example, a lead cation fraction of between about 0.20 and about 0.50, a barium cation fraction of less than about 0.26, a lanthanum cation fraction of less than about 0.05, a zinc cation fraction of between about 0.07 and about 0.17, a niobium cation fraction of between about 0.15 and about 0.33, and a titanium cation fraction of between about 0.03 and about 0.27.

An electro-optic device of the present invention may be, for example, an intensity modulator, a phase modulator, a switch, a phase retarder, a polarization controller, or a variable optical attenuator. Exemplary electro-optic devices that may be constructed using the electro-optic ceramic material of the present invention are described in U.S. Pat. No. 6,137,619, and U.S. Pat. No. 6,330,097. Electro-optic devices of the present invention may be constructed in accordance with known techniques for making devices based on other electro-optic materials, such as PLZT.

The invention will be further clarified by the following non-limiting examples which are intended to be exemplary of the invention.

EXAMPLE 1

An electro-optic ceramic material having the formula

Pb_0.83Ba_0.15La_0.02[(Zn_1/3Nb_2/3)0.7Ti_0.3]0.995O₃

was prepared using the columbite precursor—mixed oxide method as follows:

Lead (II) oxide, barium carbonate, lanthanum oxide, zinc oxide, niobium (V) oxide, and titanium (IV) oxide powders were used as starting materials. The zinc oxide and niobium (V) oxide powders (76.5 g total) were combined in amounts corresponding to the stoichiometry of the desired ceramic, and mixed with 175 mL water to form a slurry. The slurry was ball milled using 750 g alumina cylinders in a 1000 mL jar for about 30 minutes, dried at 90° C., and fired at 1000° C. for about 4 hours. The resulting solid was mixed with the stoichiometrically desired amounts of lead (II) oxide (179.9 g), barium carbonate (27.5 g), lanthanum oxide (3.1 g), and titanium (IV) oxide (22.6 g). A slight excess (about 2 wt %) of lead (II) oxide was added to counteract the effects of evaporation of lead during processing. The combined powders were mixed by ball milling for 30 minutes in a 2000 mL jar with 300 mL water and 1500 g alumina cylinders. The resulting slurry was dried at 90° C., and calcined in an alumina crucible at 900° C. for four hours. The resulting calcined powder was ball milled for 16 hours in a polyethylene jar with 300 mL trichloroethylene or acetone using alumina cylinders (1500 g) as grinding media. The resulting slurry was dried at 85° C. A one hour post annelaing step at 700° C. may be used to remove the organic residual left in the powder. An x-ray diffraction spectrum of the resulting powder is shown in FIG. 2. This spectrum indicates that the synthesized powder has an essentially pure perovskite structure. An opaque cylindrical powder preform (5.1 cm long, 3.2 cm diameter) was formed by pressing the powder in a stainless steel mold at a pressure of 2000 psi (13.793 MPa).

The powder preform 18 was loaded into a cylindrical silicon carbide mold 20 lined with a high purity alumina tube 21, as shown in FIG. 3. The silicon carbide mold had an inner diameter of 4.5 cm, and sat on an alumina pedestal 22. Two zirconium discs 23 and high purity magnesium oxide powder 24 were used to isolate the preform from the mold, the pedestal, and from the 4.5 cm diameter alumina top press rod 26. The whole assembly was mounted in a hot press machine, with the alumina top press rod being coupled to the push rod 28 a ten ton hot press from Thermal Technology Inc. of Santa Rosa, Calif. The chamber of the hot press machine was evacuated down to about 300 mTorr (40 Pa), and the temperature in the chamber was heated at a rate of about 5° C./min. When the temperature reached 650° C., oxygen was admitted to the chamber at a pressure of 3 psi (20.69 kPa). This pressure of oxygen was maintained throughout the remainder of the process. When the temperature reached 750° C., the press rod was actuated to press the preform at a pressure of 2000 psi (13.793 MPa). The preform was pressed at 1150° C. for 16 hours. The pressed slug was allowed to cool to room temperature in the press at a negligible pressure.

The slug was removed from the mold, sliced and polished. FIG. 4 shows a transmission spectrum of a 1.3 mm thick slice of Pb_0.83Ba_0.15La_0.02[(Zn_1/3Nb_2/3)_0.7Ti_0.3]_0.995O₃. The transmittance of this sample is about 70% over a wavelength range from 1300 nm to 1800 nm. The propagation loss of the material may be calculated from the transmittance using the equation $\%T={\left[1-{\left(\frac{n-1}{n+1}\right)}^2\right]}^2·{10}^{-0.1·\left[\mathrm{Propagation}\mathrm{Loss}\left(\mathrm{dB}\text{/}\mathrm{cm}\right)\right]·\left[\mathrm{Path}\mathrm{Length}\left(\mathrm{cm}\right)\right]}$

Since at 1550 nm, the refractive index of this material is about 2.3, the propagation loss of this material is less than about 1 dB/cm. The transparency of the ceramics of the present invention is comparable to the transparency of conventional PLZT materials.

Small samples of the Pb_0.83Ba_0.15La_0.02[(Zn_1/3Nb_2/3)_0.7Ti_0.3]_0.995O₃ material (5 mm×5 mm×0.7 mm) were prepared for dielectric measurements by coating with nickel electrodes. Dielectric constants were measured in an environmental chamber (from Tenney Environmental of Williamsport, Pa.) using a Model SR720 LCR meter from Stanford Research Systems of Sunnyvale, Calif. Dielectric constants at different frequencies and temperatures for this material are shown in FIG. 5. Its room temperature polarization at an electric field of 1 V/μm is 18.7 μC/cm², higher than that of PLZT under the same conditions (13.5 μC/cm²).

EXAMPLE 2

The quadratic electro-optic constant of the Pb_0.83Ba_0.15La_0.02[(Zn_1/3Nb_2/3)_{0 7}Ti_0.3]_0.995O₃ material of Example 1 was measured using the experimental setup shown in FIG. 6. Light from a fiber-pigtailed 1550 nm laser diode 40 is collimated using a GRIN lens 42, and passed through an input polarizer 44. Electrodes 46 are deposited on opposite faces of a polished sample 48 in order to allow the application of an electric field through the sample by a power source 49. The sample is placed in the light path with the direction of the applied electric field perpendicular to the direction of the light path and at a 45° angle to the polarization of the beam. After emerging from the sample the light is passed through an output polarizer 50 having its polarization axis set to be perpendicular to the polarization axis of the input polarizer 44. Light emerging from the output polarizer is coupled into a detector fiber 54 using a GRIN lens 52, and is detected by a photodetector 56. The free space portion of the setup is placed inside a temperature-controlled environmental chamber 58. A computer 60 is used to control the applied electric field, and to collect temperature and optical data. When the system is integrated with a function generator and an oscilloscope (not shown) by the skilled artisan, it may be used for measurement of response speed.

When no electric field is applied, the sample has no effect on the polarization of the beam; therefore, no light makes it to the detector due to the action of the crossed polarizers. As the applied electric field increases, the sample becomes birefringent due to the electro-optic effect, and rotates the polarization of the beam. At a voltage V_π, the polarization of the beam is rotated by the sample enough to be parallel to the polarization axis of the second polarizer, maximizing the intensity of the detected signal. Assuming the material's native birefringence (Δn₀) and linear electro-optic coefficient γ are zero, the quadratic electro-optic coefficient R may be calculated from the equation $R=\frac{{\mathrm{<figure-callout\; id="2"\; label="d"\; filenames="US06746618-20040608-D00000.png,US06746618-20040608-D00005.png"\; state="\{\{state\}\}">d</figure-callout>}}^2\mathrm{<figure-callout\; id="2"\; label="\lambda \; V\; \pi "\; filenames="US06746618-20040608-D00000.png,US06746618-20040608-D00005.png"\; state="\{\{state\}\}">\lambda </figure-callout>}}{V_{\pi }^{}}$

where d is the distance between electrodes (i.e. the width of the sample), n is the refractive index of the sample at the wavelength λ, and L is the path length of the beam in the sample.

Samples of Pb_0.83Ba_0.15La_0.02[(Zn_1/3Nb_2/3)0.7Ti_0.3]_0.995O₃ were cut from a 1.26 mm thick wafer polished on both sides. The samples had a width of 0.61 mm and a height of 2.5 mm. The parallel side surfaces of each sample were polished, plasma etched for 3 min, then coated with Pt/Au electrodes (250 Å/2500 Å). The samples were annealed at 200° C. for one hour, and at 100° C. for an additional hour to reduce the internal stresses formed in the sample preparation process. The quadratic electro-optic coefficient of the sample was measured according to the method described above to be 3.6×10⁻¹⁶ m²/V².

EXAMPLE 3

The following electro-optic ceramic materials having the formula

Pb_1−y−zBa_yLa_z[(Zn_tNb_1−t)_xTi_1−x]_1−z/4O_{3+x/2−3xt/2−xz/8+3xtz/8}

were prepared by the method of Example 1. These materials exhibited acceptable transparency for use in devices for optical telecommunications. A diagram showing these compositions graphically is given in FIG. 7.

Example	x	y	z	t

3a	0.80	0.10	0.020	1/3
3b	0.70	0.10	0.020	1/3
3c	0.782	0.15	0.020	1/3
3d	0.70	0.15	0.020	1/3
3e	0.65	0.15	0.020	1/3
3f	0.70	0.20	0.020	1/3
3g	0.60	0.20	0.020	1/3

Transmission spectra of 1.44 mm thick slabs of the materials of Examples 3c and 3d are given in FIG. 8. A plot of quadratic electro-optic coefficient vs. temperature of the material of Example 3d was collected according to Example 2, and is shown in FIG. 9.

It will be apparent to those skilled in the art that various modifications and variations can be made to the present invention without departing from the spirit and scope of the invention. Thus, it is intended that the present invention covers the modifications and variations of this invention provided they come within the scope of the appended claims and their equivalents.

Claims (21)

What is claimed is:

1. A lanthanum containing, lead zinc niobate-based electro-optic ceramic material having a propagation loss of less than about 3 dB/cm and a quadratic electro-optic coefficient of greater than about 1×10⁻¹⁶ m²/V² at 20° C. at a wavelength of 1550 nm.

2. The electro-optic ceramic material of claim 1 wherein the propagation loss of the material is less than about 1.5 dB/cm at a wavelength of 1550 nm.

3. The electro-optic ceramic material of claim 1 wherein the material has a quadratic electro-optic coefficient at 20° C. at 1550 nm of greater than about 3×10⁻¹⁶ m²/V².

4. The electro-optic ceramic material of claim 1 further comprising barium.

5. The electro-optic ceramic material of claim 1 further comprising titanium, wherein the electro-optic ceramic material has

a lead cation fraction of between about 0.20 and about 0.50;

a barium cation fraction of less than about 0.26;

a lanthanum cation fraction of less than about 0.05;

a zinc cation fraction of between about 0.07 and about 0.17;

a niobium cation fraction of between about 0.15 and about 0.33; and

a titanium cation fraction of between about 0.03 and about 0.27.

6. The electro-optic ceramic material of claim 5, wherein the electro-optic ceramic material has a lead cation fraction of between about 0.37 and about 0.45.

7. The electro-optic ceramic material of claim 5 wherein the electro-optic ceramic material has a barium cation fraction of between about 0.04 and about 0.11.

8. The electro-optic ceramic material of claim 5 wherein the electro-optic ceramic material has a lanthanum cation fraction of between about 0.01 and about 0.04.

9. The electro-optic ceramic material of claim 5 wherein the electro-optic ceramic material has a zinc cation fraction of between about 0.10 and about 0.15.

10. The electro-optic ceramic material of claim 5 wherein the electro-optic ceramic material has a niobium cation fraction of between about 0.20 and about 0.29.

11. The electro-optic ceramic material of claim 5 wherein the electro-optic ceramic material has a titanium cation fraction of between about 0.07 and about 0.18.

12. The electric optic ceramic material of claim 1 wherein the electro-optic ceramic material has the formula

Pb_1−y−zBa_yLa_z[(Zn_tNb_1−t)_xTi_1−x]_1−z/4O_{3+x/2−3xt/2−xz/8+3xtz/8}

wherein

x is between about 0.5 and about 0.9,

y is between about 0.05 and about 0.5,

z is between about 0 and about 0.05,

t is between about 0.30 and about 0.36, and

wherein the material has a propagation loss of less than about 3 dB/cm and a quadratic electro-optic coefficient of greater than about 1×10⁻¹⁶ m²/V² at 20° C. at a wavelength of 1550 nm.

13. The electro-optic ceramic material of claim 12 wherein x is between about 0.65 and about 0.85.

14. The electro-optic ceramic material of claim 12 wherein y is between about 0.1 and about 0.2.

15. The electro-optic ceramic material of claim 12 wherein z is between about 0.02 and about 0.04.

16. The electro-optic ceramic material of claim 12 wherein t is between about 0.32 and about 0.34.

17. An electro-optic device comprising a lanthanum containing, lead zinc niobate-based electro-optic ceramic material having a propagation loss of less than about 3 dB/cm and a quadratic electro-optic coefficient of greater than about 1×10⁻¹⁶ m²/V² at 20° C. at a wavelength of 1550 nm.

18. The electro-optic device of claim 17 wherein the electro-optic ceramic material has a propagation loss of less than about 1.5 dB/cm at a wavelength of 1550 nm.

19. The electro-optic device of claim 17 wherein the electro-optic ceramic material has a quadratic electro-optic coefficient of greater than about 3×10¹⁶ m²/V² at 20° C. at a wavelength of 1550 nm.

20. The electro-optic device of claim 17 wherein the electro-optic ceramic material further comprises titanium, and wherein the electro-optic ceramic material has

a lead cation fraction of between about 0.20 and about 0.50;

a barium cation fraction of less than about 0.26;

a lanthanum cation fraction of less than about 0.05;

a zinc cation fraction of between about 0.07 and about 0.17;

a niobium cation fraction of between about 0.15 and about 0.33; and

a titanium cation fraction of between about 0.03 and about 0.27.

21. The electro-optic device of claim 17 wherein the electro-optic device is selected from the group consisting of an intensity modulator, a phase modulator, a switch, a phase retarder, a polarization controller, and a variable optical attenuator.

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